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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Autoplak — 3 UDI-DI variants, IVDR (SENER Diagnostics S.A.)

MD Atlas
SENER Diagnostics S.A.

Data from EUDAMED, last updated May 23, 2026

Autoplak

8437024289Autoplak01BG

3 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: SENER Diagnostics S.A.

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 8437024289Autoplak01BG
Device name: Autoplak
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Apr 15, 2024

Manufacturer & authorised representative

Manufacturer

Name: SENER Diagnostics S.A.
SRN: ES-MF-000030726
Country: Spain
Email: eva.creus@aeroespacial.sener
Phone: +34932283300

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HVGQ4WS3T6RJS349PK23C0K9

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Autoplak Complete 08437024289005
Autoplak Advance08437024289012
Autoplak Advance ETL08437024289029